Ohmic contact to semiconductor device

ABSTRACT

Embodiments of an ohmic contact structure for a Group III nitride semiconductor device and methods of fabrication thereof are disclosed. In one embodiment, the ohmic contact structure has less than or equal to 5%, more preferably less than or equal to 2%, more preferably less than or equal to 1.5%, and even more preferably less than or equal to 1% degradation for 1000 hours High Temperature Soak (HTS) at 300 degrees Celsius. In another embodiment, the ohmic contact structure additionally or alternatively has less than or equal to 10% degradation, more preferably less than or equal to 7.5% degradation, more preferably less than or equal to 6% degradation, more preferably less than or equal to 5% degradation, and even more preferably less than 3% degradation for 1000 hours High Temperature operating Life (HToL) at 225 degrees Celsius and 50 milliamps (mA) per millimeter (mm).

RELATED APPLICATIONS

This application is a continuation-in-part of co-pending U.S. patent application Ser. No. 12/704,013 entitled METHODS OF FORMING CONTACT STRUCTURES INCLUDING ALTERNATING METAL AND SILICON LAYERS AND RELATED DEVICES, filed on Feb. 11, 2010, assigned to the assignee of the present application, and incorporated herein by reference in its entirety.

GOVERNMENT SUPPORT

This invention was made with government funds under contract number 05-D-6000 awarded by NAVSEA. The U.S. Government may have rights in this invention.

FIELD OF THE DISCLOSURE

The present disclosure relates to ohmic contacts for semiconductor devices.

BACKGROUND

Materials such as silicon (Si) and gallium arsenide (GaAs) have found wide application in semiconductor devices for lower power and (in the case of Si) lower frequency applications. These more familiar semiconductor materials may not be well suited for high power and/or high frequency applications, however, because of their relatively small bandgaps (e.g., 1.12 electron volts (eV) for Si and 1.42 eV for GaAs at room temperature) and/or relatively small breakdown voltages.

In light of the difficulties presented by Si and GaAs, interest in high power, high temperature and/or high frequency applications and devices has turned to wide bandgap semiconductor materials such as silicon carbide (2.996 eV for alpha SiC at room temperature) and the Group III nitrides (e.g., 3.36 eV for GaN at room temperature). These materials, typically, have higher electric field breakdown strengths and higher electron saturation velocities as compared to GaAs and Si.

In Group III nitride semiconductor devices, as with semiconductor devices fabricated in other material systems, low-resistance, stable ohmic contacts are critical for the performance and reliability of the semiconductor devices. Thus, there is a need for improved ohmic contact structures and methods of fabrication thereof for Group III nitride semiconductor devices.

SUMMARY

Embodiments of an ohmic contact structure for a Group III nitride semiconductor device and methods of fabrication thereof are disclosed. In one embodiment, the ohmic contact structure has less than or equal to 5%, more preferably less than or equal to 2%, more preferably less than or equal to 1.5%, and even more preferably less than or equal to 1% degradation for 1000 hours High Temperature Soak (HTS) at 300 degrees Celsius. In another embodiment, the ohmic contact structure additionally or alternatively has less than or equal to 10% degradation, more preferably less than or equal to 7.5% degradation, more preferably less than or equal to 6% degradation, more preferably less than or equal to 5% degradation, and even more preferably less than or equal to 3% degradation for 1000 hours High Temperature operating Life (HToL) at 225 degrees Celsius and 50 milliamps (mA) per millimeter (mm).

In one embodiment, the ohmic contact structure includes a titanium layer on a surface of a Group III nitride semiconductor structure, a nickel silicide layer on a surface of the titanium layer opposite the surface of the Group III nitride semiconductor structure, and a metal cap layer on a surface of the nickel silicide layer opposite the Group III nitride semiconductor layer. In one embodiment, the Group III nitride semiconductor structure includes gallium nitride (GaN) and/or aluminum gallium nitride (AlGaN). The titanium layer, the nickel silicide layer, and the metal cap layer are selectively formed such that the ohmic contact structure has less than or equal to 5%, more preferably less than or equal to 2%, more preferably less than or equal to 1.5%, and even more preferably less than or equal to 1%, degradation for 1000 hours HTS at 300 degrees Celsius and/or less than or equal to 10%, more preferably less than or equal to 7.5% degradation, more preferably less than or equal to 6% degradation, more preferably less than or equal to 5% degradation, and even more preferably less than or equal to 3% degradation for 1000 hours HToL at 225 degrees Celsius and 50 mA/mm. The metal cap layer may be formed of, for example, tellurium (Te), platinum (Pt), palladium (Pd), vanadium (V), tungsten (W), gold (Au), iridium (Ir), or rhodium (Rh).

In another embodiment, the ohmic contact structure includes a titanium layer of a surface of a Group III nitride semiconductor structure, an alternating series of one or more silicon layers and one or more nickel layers on a surface of the titanium layer opposite the surface of the Group III nitride semiconductor structure, and a metal cap layer on a surface of the alternating series of one or more silicon layers and one or more nickel layers opposite the surface of the titanium layer. In one embodiment, the alternating series of one or more silicon layers and one or more nickel layers includes one silicon layer and one nickel layer. In another embodiment, the alternating series of one or more silicon layers and one or more nickel layers includes two or more silicon layers and two or more nickel layers. The ohmic contact structure is thermally annealed such that the one or more silicon layers and the one or more nickel layers form a nickel silicide layer. In one embodiment, the Group III nitride semiconductor structure includes GaN and/or AlGaN. The titanium layer, the alternating series of one or more silicon layers and one or more nickel layers, and the metal cap layer are selectively formed such that the ohmic contact structure has less than or equal to 5%, more preferably less than or equal to 2%, more preferably less than or equal to 1.5%, and even more preferably less than or equal to 1%, degradation for 1000 hours HTS at 300 degrees Celsius and/or less than or equal to 10%, more preferably less than or equal to 7.5% degradation, more preferably less than or equal to 6% degradation, more preferably less than or equal to 5% degradation, and even more preferably less than or equal to 3% degradation for 1000 hours HToL at 225 degrees Celsius and 50 mA/mm. The metal cap layer may be formed of, for example, Te, Pt, Pd, V, W, Au, Ir, or Rh.

Those skilled in the art will appreciate the scope of the present disclosure and realize additional aspects thereof after reading the following detailed description of the preferred embodiments in association with the accompanying drawing figures.

BRIEF DESCRIPTION OF THE DRAWING FIGURES

The accompanying drawing figures incorporated in and forming a part of this specification illustrate several aspects of the disclosure, and together with the description serve to explain the principles of the disclosure.

FIGS. 1 through 4 are cross sectional views illustrating operations of forming ohmic contact structures according to some embodiments of the present disclosure;

FIG. 5 is a greatly enlarged cross sectional view of an ohmic contact structure on a substrate as shown in FIGS. 1 and 2;

FIG. 6 is a graph illustrating sheet resistances of ohmic contact structures;

FIG. 7 illustrates an ohmic contact structure for a Group Ill nitride semiconductor device according to one embodiment of the present disclosure;

FIGS. 8A through 8F graphically illustrate fabrication of the ohmic contact structure of FIG. 7 according to one embodiment of the present disclosure;

FIG. 9 illustrates an ohmic contact structure for a Group Ill nitride semiconductor device according to another embodiment of the present disclosure;

FIGS. 10A and 10B illustrate data and a corresponding graph showing percent degradation of an exemplary embodiment of the ohmic contact of FIG. 7 after 1000 hours High Temperature Soak (HTS) at 300 degrees Celsius;

FIGS. 11A and 11B illustrate data and a corresponding graph showing percent degradation of an exemplary embodiment of the ohmic contact of FIG. 9 after 1000 hours HTS at 300 degrees Celsius; and

FIGS. 12A and 12B illustrate data and a corresponding graph showing percent degradation of an exemplary embodiment of the ohmic contact of FIGS. 7 and 9 after 1000 hours High Temperature operating Life (HToL) at 225 degrees Celsius and 50 milliamps (mA) per millimeter (mm).

DETAILED DESCRIPTION

The embodiments set forth below represent the necessary information to enable those skilled in the art to practice the embodiments and illustrate the best mode of practicing the embodiments. Upon reading the following description in light of the accompanying drawing figures, those skilled in the art will understand the concepts of the disclosure and will recognize applications of these concepts not particularly addressed herein. It should be understood that these concepts and applications fall within the scope of the disclosure and the accompanying claims.

It will be understood that, although the terms first, second, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another. For example, a first element could be termed a second element, and, similarly, a second element could be termed a first element, without departing from the scope of the present disclosure. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.

It will be understood that when an element such as a layer, region, or substrate is referred to as being “on” or extending “onto” another element, it can be directly on or extend directly onto the other element or intervening elements may also be present. In contrast, when an element is referred to as being “directly on” or extending “directly onto” another element, there are no intervening elements present. It will also be understood that when an element is referred to as being “connected” or “coupled” to another element, it can be directly connected or coupled to the other element or intervening elements may be present. In contrast, when an element is referred to as being “directly connected” or “directly coupled” to another element, there are no intervening elements present.

Relative terms such as “below” or “above” or “upper” or “lower” or “horizontal” or “vertical” may be used herein to describe a relationship of one element, layer, or region to another element, layer, or region as illustrated in the Figures. It will be understood that these terms and those discussed above are intended to encompass different orientations of the device in addition to the orientation depicted in the 1s.

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the disclosure. As used herein, the singular forms “a,” “an,” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises,” “comprising,” “includes,” and/or “including” when used herein specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof.

Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. It will be further understood that terms used herein should be interpreted as having a meaning that is consistent with their meaning in the context of this specification and the relevant art and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.

Embodiments are described herein with reference to cross-sectional illustrations that are schematic illustrations of idealized embodiments (and intermediate structures). The thickness of layers and regions in the drawings may be exaggerated for clarity. Additionally, variations from the shapes of the illustrations as a result, for example, of manufacturing techniques and/or tolerances, are to be expected. Thus, the embodiments described herein should not be construed as limited to the particular shapes of regions illustrated herein but are to include deviations in shapes that result, for example, from manufacturing. For example, an implanted region illustrated as a rectangle will, typically, have rounded or curved features and/or a gradient of implant concentration at its edges rather than a discrete change from implanted to non-implanted region. Likewise, a buried region formed by implantation may result in some implantation in the region between the buried region and the surface through which the implantation takes place. Thus, the regions illustrated in the figures are schematic in nature and their shapes are not intended to illustrate the actual shape of a region of a device and are not intended to limit the scope of the disclosure.

Some embodiments of the disclosure are described with reference to semiconductor layers and/or regions which are characterized as having a conductivity type such as N type or P type, which refers to the majority carrier concentration in the layer and/or region. Thus, N type material has a majority equilibrium concentration of negatively charged electrons, while P type material has a majority equilibrium concentration of positively charged holes. Some material may be designated with a “⁺” or “⁻” (as in N⁺, N⁻, P³⁰ , P³¹ , N⁺⁺, N⁻⁻, P⁺⁺, P⁻⁻, or the like), to indicate a relatively larger (“⁺”) or smaller (“⁻”) concentration of majority carriers compared to another layer or region. However, such notation does not imply the existence of a particular concentration of majority or minority carriers in a layer or region.

Silicon carbide (SiC) substrates/layers discussed herein may be 4H polytype silicon carbide substrates/layers. Other SiC candidate polytypes, such as 3C, 6H, and 15R polytypes, however, may be used. Appropriate SiC substrates are available from Cree Research, Inc., of Durham, N.C., the assignee of the present invention, and the methods for producing such substrates are set forth in the scientific literature as well as in a number of commonly assigned U.S. Patents, including but not limited to U.S. Pat. No. RE34,861, U.S. Pat. No. 4,946,547, and U.S. Pat. No. 5,200,022, the disclosures of which are incorporated herein in their entirety by reference.

As used herein, the term “Group III nitride” refers to those semiconducting compounds formed between nitrogen and one or more elements in Group III of the periodic table, usually aluminum (Al), gallium (Ga), and indium (In). The term also refers to binary, ternary, and quaternary compounds such as GaN, AlGaN and AlInGaN. The Group III elements can combine with nitrogen to form binary (e.g., GaN), ternary (e.g., AlGaN), and quaternary (e.g., AlInGaN) compounds. These compounds may have empirical formulas in which one mole of nitrogen is combined with a total of one mole of the Group III elements. Accordingly, formulas such as Al_(x)Ga_(1-x)N where 1>x>0 are often used to describe these compounds. Techniques for epitaxial growth of Group III nitrides have become reasonably well developed and reported in the appropriate scientific literature, and in commonly assigned U.S. Pat. No. 5,210,051, U.S. Pat. No. 5,393,993, and U.S. Pat. No. 5,523,589, the disclosures of which are hereby incorporated herein in their entirety by reference.

A contact structure for a semiconductor device may provide ohmic contact with an underlying semiconductor material. In a Group III nitride semiconductor device, such as a High Electron Mobility Transistor (HEMT), a source/drain contact may provide ohmic contact with a 2 Dimensional Electron Gas (2 DEG) in a Group III nitride semiconductor material(s) such as gallium nitride (GaN), aluminum gallium nitride, indium gallium nitride, indium nitride, indium aluminum nitride, and/or indium gallium aluminum nitride. While aluminum-nickel structures may provide ohmic contact with Group III nitride semiconductor materials, an aluminum-nickel structure may be subject to galvanic corrosion, chemical attack during subsequent etching, and/or adhesion problems.

According to some embodiments of the present disclosure, a source/drain contact for a semiconductor layer may include a layer of a first metal on the semiconductor layer and a silicide layer including a second metal (i.e., a silicide of the second metal) on the layer of the first metal, with the first and second metals being different. For example, the first metal may be titanium and/or any other suitable metal, and the second metal may be nickel and/or any other suitable metal. More particularly, alternating layers of silicon and the second metal may be formed on the layer of the first metal and then annealed to form the silicide layer. In addition, a layer of a third metal may be formed on the alternating layers of silicon and the second metal before annealing to thereby reduce oxidation of the contact structure. The third metal may be gold, platinum, palladium, and/or any other suitable metal. The resulting ohmic contact structure may be chemically stable and/or corrosion resistant, and/or may provide a low resistance contact with the underlying semiconductor layer while maintaining adhesion with the underlying semiconductor layer over a useful life of the device.

FIGS. 1 to 4 are cross sectional views illustrating operations of forming ohmic contact structures according to embodiments of the present disclosure. As shown in FIG. 1, a semiconductor structure 103, such as a semiconductor structure for a Group III nitride semiconductor HEMT (High Electron Mobility Transistor), may be formed on a substrate 101 such as a silicon carbide (SiC) substrate or a sapphire substrate. The substrate 101 may be a semi-insulating silicon carbide (SiC) substrate that may be, for example, the 4H polytype of silicon carbide. Other silicon carbide candidate polytypes may include the 3C, 6H, and 15R polytypes. The substrate 101 may be a High Purity Semi-Insulating (HPSI) substrate, available from Cree, Inc. The term “semi-insulating” is used descriptively herein, rather than in an absolute sense.

In some embodiments of the present disclosure, the silicon carbide bulk crystal may have a resistivity equal to or higher than about 1×10⁵ ohm-cm at room temperature. Exemplary SiC substrates that may be used in some embodiments of the present disclosure are manufactured by, for example, Cree, Inc., of Durham, N.C., the assignee of the present disclosure, and methods for producing such substrates are described, for example, in U.S. Pat. No. RE34,861, U.S. Pat. No. 4,946,547, U.S. Pat. No. 5,200,022, and U.S. Pat. No. 6,218,680, the disclosures of which are incorporated by reference herein in their entireties. Similarly, techniques for epitaxial growth of Group III nitrides have been described in, for example, U.S. Pat. No. 5,210,051, U.S. Pat. No. 5,393,993, and U.S. Pat. No. 5,523,589, the disclosures of which are also incorporated by reference herein in their entireties.

Semiconductor structure 103 may include a channel layer 103 a and a barrier layer 103 b formed of Group III nitride semiconductor materials having different bandgaps, such that an interface between the channel layer 103 a and the barrier layer 103 b defines a heterojunction. Channel layer 103 a may be a Group III nitride layer, such as GaN. Channel layer 103 a may also include other Group III nitride layers, such as indium gallium nitride (InGaN), aluminum indium gallium nitride (AlInGaN), or the like. Channel layer 103 a may be undoped (i.e., “unintentionally doped”), and may be grown to a thickness of greater than about 20 Angstroms. Channel layer 103 a may also be a multi-layer structure, such as a superlattice or combinations of GaN, AlGaN, or the like.

Barrier layer 103 b may be a Group III nitride layer, such as Al_(x)Ga_(1-x)N (where 0<x<1). The barrier layer 103 b may also include other Group III nitride layers, such as AlInGaN, AlN, and/or combinations of layers thereof. Barrier layer 103 b may, for example, be from about 0.1 nanometer (nm) to about 100 nm thick, but may be thin enough to reduce substantial cracking and/or defect formation therein. In some embodiments of the present disclosure, the barrier layer 103 b may be a highly-doped n-type layer. For example, the barrier layer 103 b may be doped to a concentration of about 10¹⁹ cm⁻³. While semiconductor structure 103 is shown with channel layer 103 a and barrier layer 103 b for purposes of illustration, semiconductor structure 103 may include additional layers/structures/elements such as a buffer and/or nucleation layer(s) between channel layer 103 a and substrate 101, and/or a cap layer on barrier layer 103 b. HEMT structures including substrates, channel layers, barrier layers, and other layers are discussed by way of example in U.S. Pat. No. 5,192,987, U.S. Pat. No. 5,296,395, U.S. Pat. No. 6,316,793, U.S. Pat. No. 6,548,333, U.S. Pat. No. 7,544,963, U.S. Pat. No. 7,548,112, U.S. Pat. No. 7,592,211, U.S. Publication No. 2006/0244010, U.S. Publication No. 2007/0018210, and U.S. Publication No. 2007/0164322, the disclosures of which are hereby incorporated herein in their entirety by reference.

As further shown in FIG. 1, a photoresist lift-off mask 105 may be formed on semiconductor structure 103, exposing portions of semiconductor structure 103 where ohmic contacts will be formed. Then, layers of ohmic contact materials may be formed on photoresist lift-off mask 105 and on exposed portions of semiconductor structure 103 to provide the structure shown in FIG. 1. More particularly, a layer 107 of a first metal may be formed on photoresist lift-off mask 105 and on exposed portions of semiconductor structure 103, and alternating layers 109 of silicon and a second metal may be formed on layer 107 of the first metal. In addition, a layer 111 of a third metal may be formed on alternating layers 109 of silicon and the second metal. By way of example, layer 107 may be a layer of titanium (Ti) and/or any other suitable metal, alternating layers 109 may be alternating layers of silicon (Si) and nickel (Ni) (and/or any other suitable metal), and layer 111 may be a layer of gold (Au), platinum (Pt), palladium (Pd) and/or any other suitable metal. Moreover, layer 107, alternating layers 109, and cap layer 111 may be formed in situ in a same reaction chamber, for example, by evaporation. In addition, semiconductor structure 103 may include doped source/drain regions 106 providing electrical coupling between respective layers 107 of the first metal and a 2 DEG at an interface between channel and barrier layers 103 a and 103 b. Doped source/drain regions 106, for example, may be doped to provide n-type conductivity.

FIG. 5 is a greatly enlarged cross sectional view illustrating portions of layers 107, 109 and 111 on a portion of semiconductor structure 103. In particular, layer 107 of the first metal may be formed directly on a Group III semiconductor nitride layer (such as an AlGaN layer) of semiconductor structure 103, and alternating layers 109 a of silicon and 109 b of the second metal may be formed on layer 107 of the first metal. As shown in FIG. 5 a first of silicon layers 109 a may separate all of layers 109 b of the second metal from layer 107 of the first metal. More particularly, a first of silicon layers 109 a may be directly on layer 107 of the first metal. According to some embodiments of the present disclosure, silicon layers 109 a may be thicker than adjacent layers 109 b of the second metal, and more particularly, thicknesses of silicon layers 109 a may be about 2 times greater than thickness of adjacent layers 109 b of the second metal.

According to particular embodiments of the present disclosure, layer 107 may be a layer of titanium, layers 109 a may be layers of silicon, and layers 109 b may be layers of nickel. Thicknesses of silicon layers 109 a may be in the range of about 400 Angstroms to about 600 Angstroms and thicknesses of layers 109 b of nickel may be in the range of about 200 Angstroms to about 300 Angstroms, and more particularly, thicknesses of silicon layers 109 a may be about 500 Angstroms and thicknesses of layers 109 b of nickel may be about 250 Angstroms. More generally, thickness of layers 109 a and 109 b may be selected to provide in the range of about 45 to about 55 atomic weight percent of silicon in the combination of alternating layers 109, and more particularly, in the range of about 48 to about 52 atomic weight percent of silicon. According to some embodiments of the present disclosure, thicknesses of layers 109 a and 109 b may be selected to provide about 50 atomic weight percent of silicon in the combination of alternating layers 109 of silicon and nickel.

Alternating layers 109 a and 109 b may include at least one layer 109 a of silicon and at least one layer 109 b of nickel to provide at least one pair of silicon and nickel layers 109 a and 109 b. According to some embodiments of the present disclosure, between two and ten pairs of silicon and nickel layers 109 a and 109 b may be included in stack 109, and according to particular embodiments, three or four pairs of silicon and nickel layers 109 a and 109 b may be provided. According to other embodiments of the present disclosure, at least two pairs of silicon and nickel layers 109 a and 109 b may be included. While pairs of silicon and nickel layers are shown by way of example, a last nickel layer may be omitted so that there is one more silicon layer than nickel layer. According to some embodiments of the present disclosure, a single layer 109 b of the second metal may be sandwiched between two layers 109 a of silicon.

In addition, a cap layer 111 may be provided on the alternating layers 109 so that the alternating layers 109 are sandwiched between cap layer 111 and titanium layer 107. Cap layer 111, for example, may be a layer of gold, palladium, and/or platinum, and cap layer 111 may have a thickness of less than about 500 Angstroms, and more particularly, in the range of about 50 Angstroms to about 200 Angstroms. According to other embodiments of the present disclosure, cap layer 111 may be omitted. Cap layer 111, for example, may reduce oxidation of alternating layers 109 and/or of a subsequently formed silicide.

As shown in FIG. 2, photoresist lift-off mask 105 and portions of layers 107, 109, and 111 thereon may be removed. Accordingly, separate ohmic contact structures 115 (including respective layer 107 of the first metal, alternating layers 109, and cap layer 111) may remain on semiconductor structure 103 having the structure of FIG. 5. While lift-off patterning is discussed by way of example in FIGS. 1 and 2, ohmic contact structures 115 may be formed using other operations. For example, blanket layers 107, 109, and 111 may be formed directly on semiconductor structure 103 (i.e., without a photoresist lift-off mask), and then patterned using subsequent photolithographic masking and etch operations.

The alternating layers 109 may then be subjected to a thermal annealing operation to provide a contact structures 115′ including silicide layer 109′ of the second metal (e.g., nickel silicide and/or any other suitable metal silicide) on layer 107 of the first metal. More particularly, the thermal anneal may be performed at a temperature sufficient to form the silicide including the second metal (e.g., nickel and/or any other suitable metal) without forming significant silicide of the first metal (e.g., titanium and/or any other suitable metal). Moreover, by providing a first of silicon layers 109 a between all of the layers 109 b of the second metal and layer 107 of the first metal, mixing of the first and second metals during the thermal annealing operation may be reduced. By way of example, with a titanium layer 107 and nickel layers 109 b, a rapid thermal anneal (RTA) may be performed at a temperature that does not exceed about 500 degrees C. to form nickel silicide without significant mixing of titanium and nickel and without significant formation of titanium silicide. The rapid thermal anneal, for example, may be performed at a temperature in the range of about 200 degrees C. to about 500 degrees C.

Moreover, by providing appropriate thicknesses of layers 109 a and 109 b as discussed above, an atomic weight percent of silicon in the resulting silicide layer 109′ may be in the range of about 45 to about 55 atomic weight percent, and more particularly, the range of about 48 to about 52 atomic weight percent. According to some embodiments of the present disclosure, an atomic weight percent of silicon in the resulting silicide layer 109′ may be about 50 atomic weight percent. Moreover, a composition of the metal silicide may be relatively uniform throughout a thickness of silicide layer 109′. In addition, cap layer 111 (if included) may reduce oxidation of alternating layers 109 and/or silicide layer 109′ before/during/after the thermal annealing operation.

In addition, protective layer 117 may be formed on contact structures 115′ before or after the thermal anneal operation as further shown in FIG. 3. Protective layer 117, for example, may be a layer of an insulating material such as silicon nitride (Si_(x)N_(y)), aluminum nitride (AlN), silicon dioxide (SiO₂), and/or other suitable protective material. Other materials may also be used for the protective layer 117. For example, protective layer 117 may also include magnesium oxide, scandium oxide, aluminum oxide and/or aluminum oxynitride. Furthermore, protective layer 117 may be a single layer or may include multiple layers of uniform and/or non-uniform composition.

While cap layer 111 is shown after forming protective layer 117 in FIG. 3 by way of example, cap layer 111 may be removed after the thermal anneal operation and before forming protective layer 117. Moreover, protective layer 117 may be omitted altogether as discussed above.

Protective layer 117 may then be patterned using photolithographic mask and etch operations as shown in FIG. 4 to expose contact structures 115′ and to expose a gate contact area 119 of semiconductor structure 103. Source/drain electrodes 121 and gate electrode 123 may then be formed as further shown in FIG. 4. According to some embodiments of the present disclosure, source/drain electrodes 121 and gate electrode 123 may be formed at the same time using a same material such as gold and/or any other suitable metal. For example, a blanket layer of a metal (e.g., gold and/or any other suitable metal) may be deposited and then patterned using subsequent photolithographic mask and etch operations to form source/drain electrodes and gate electrode 123. According to other embodiments of the present disclosure, gate electrode 123 (or portions thereof) may be formed separately from source/drain electrodes 121 so that gate electrode 123 and source/drain electrodes may comprise different materials. While gold is discussed by way of example as a gate electrode material, other materials, such as nickel, platinum, nickel silicide, copper, palladium, chromium, tungsten, tungsten silicon nitride, and/or any other suitable conductive material may be used for gate electrode 123. According to some embodiments of the present disclosure, portions of gate electrode 123 may directly contact semiconductor structure 103 to provide a Schottky or otherwise non-ohmic contact therebetween. Accordingly, a material of gate electrode 123 may be selected to provide such a Schottky or other non-ohmic contact with gate contact area 119 of semiconductor structure 103.

According to some embodiments of the present disclosure, gate electrode 123 may be formed, and then a layer of metal for source/drain electrodes 121 may be formed/patterned to provide source/drain electrodes 121. While not shown in FIG. 4, an insulating layer may be formed on gate electrode 123, on ohmic contacts 115′, and on protective layer 117. This insulating layer may be patterned to expose portions of ohmic contacts 115′, and then source/drain electrodes 121 may be formed on this insulating layer and on exposed portions of respective ohmic contacts 115′.

As shown in FIG. 4, cap layers 111 may be maintained on ohmic contacts 115′ after forming source/drain electrodes 121. According to other embodiments of the present disclosure, cap layers 111 may be removed after patterning protective layer 117 and before forming source/drain electrodes 121. According to still other embodiments of the present disclosure, cap layer 111 may be removed prior to forming protective layer 117 or omitted altogether as discussed above with respect to FIGS. 1-3.

The HEMT of FIG. 4 may thus provide conduction between ohmic contacts 115′ through a 2-dimensional electron gas (2 DEG) at an interface between channel layer 103 a and barrier layer 103 b. Moreover, conduction through the 2 DEG between ohmic contacts 115′ may be modulated responsive to an electrical signal applied to gate electrode 123.

Ohmic contact structures and methods of fabrication have been discussed above by way of example with respect to Group III nitride semiconductor HEMT structures. Ohmic contact structures and methods according to embodiments of the present disclosure may be used with other semiconductor devices and/or materials. Ohmic contact structures and methods according to other embodiments of the present disclosure, for example, may be used with MOSFET transistors, with bipolar junction transistors, with light emitting diodes, etc. Moreover, ohmic contact structures and methods according to embodiments of the present disclosure may be used with horizontal devices having all contacts on a same side/face of the device as discussed above with respect to FIGS. 1-4 or with vertical devices having contacts on opposite sides/faces of the device.

FIG. 6 is a graph illustrating average sheet resistances (measured in ohms/square) and ranges thereof for ohmic contact structures fabricated on different wafers. The NiSi_B group includes three wafers (HP0217-10, HP0221-06, and KC0034-04) provided with ohmic contact structures formed according to embodiments of the present disclosure as shown in FIGS. 1-5, with each ohmic contact structure including a titanium layer and a silicide layer formed by annealing three layers of silicon (each having a thickness of about 500 Angstroms) alternating with three layers of nickel (each having a thickness of about 250 Angstroms). The NiSiA group includes three wafers (HP0220-11, HP0221-09, and HP0222-02) provided with ohmic contact structures formed according to embodiments of the present disclosure as shown in FIGS. 1-5, with each ohmic contact structure including a titanium layer and a silicide layer formed by annealing two layers of silicon (each having a thickness of about 500 Angstroms) alternating with two layers of nickel (each having a thickness of about 250 Angstroms). The Ti/Al/Ni comparison group includes four wafers (FM0562-05, GF0301-07, GF0329-12, and JS0077-02) provided with ohmic contact structures, with each ohmic contact structure formed from layers including a titanium layer, an aluminum layer, and a nickel layer.

As shown in the graph of FIG. 6, resistances of ohmic contact structures of the NiSi_B group according to embodiments of the present disclosure and the Ti/Al/Ni comparison group may be statistically very similar. As noted above, however, ohmic contact structures including silicides formed by annealing alternating layers of silicon and nickel may provide increased resistance to damage from subsequent etch operations, reduced damage from corrosion, and/or improved adhesion.

FIGS. 7 through 9 describe embodiments of an ohmic contact structure for a Group III nitride semiconductor device, and methods of fabrication thereof, that in one embodiment have less than or equal to 5%, more preferably less than or equal to 2%, more preferably less than or equal to 1.5%, and even more preferably less than or equal to 1%, degradation for 1000 hours High Temperature Soak (HTS) at 300 degrees Celsius. In another embodiment, the ohmic contact structures of FIGS. 7 through 9 additionally or alternatively have less than or equal to 10%, more preferably less than or equal to 7.5%, more preferably less than or equal to 6%, more preferably less than or equal to 5%, and even more preferably less than or equal to 3% degradation for 1000 hours High Temperature operating Life (HToL) at 225 degrees Celsius and 50 milliamps (mA) per millimeter (mm).

FIG. 7 illustrates an ohmic contact structure 125 on a GaN/Aluminum Gallium Nitride (AlGaN) structure 127 according to one embodiment of the present disclosure. The GaN/AlGaN structure 127 includes one or more layers of GaN and/or AlGaN in which one or more semiconductor devices are formed. The semiconductor devices may be, for example, HEMTs, MOSFETs, PIN diodes, bipolar junction transistors, light emitting diodes, or the like. However, one of skill in the art will readily appreciate that other types of semiconductor devices may be fabricated in the GaN/AlGaN structure 127.

Note that while the GaN/AlGaN structure 127 is shown, other Group III nitride semiconductor structures may be used. As used herein, the term “Group III nitride” refers to those semiconducting compounds formed between nitrogen and one or more elements in Group III of the periodic table, usually aluminum (Al), gallium (Ga), and indium (In). The term also refers to binary, ternary, and quaternary compounds such as GaN, AlGaN, and AlInGaN. The Group III elements can combine with nitrogen to form binary (e.g., GaN), ternary (e.g., AlGaN), and quaternary (e.g., AlInGaN) compounds. These compounds may have empirical formulas in which one mole of nitrogen is combined with a total of one mole of the Group III elements. Accordingly, formulas such as Al_(x)Ga_(1-x)N where 1>x>0 are often used to describe these compounds. Techniques for epitaxial growth of Group III nitrides have become reasonably well developed and reported in the appropriate scientific literature, and in commonly assigned U.S. Pat. No. 5,210,051, U.S. Pat. No. 5,393,993, and U.S. Pat. No. 5,523,589, the disclosures of which are hereby incorporated herein by reference in their entireties. It should also be noted that while the present disclosure focuses on the GaN/AlGaN structure 127 and similar Group III nitride semiconductor structures, similar ohmic contact structures may be utilized for other types of semiconductor structures such as, for example, SiC semiconductor structures.

In this embodiment, the ohmic contact structure 125 includes a titanium metal layer 129 on a surface of the GaN/AlGaN structure 127; a nickel silicide (NiSi) layer 131 formed by thermally annealing a silicon layer 133 on a surface of the titanium metal layer 129 opposite the GaN/AlGaN structure 127 and a nickel layer 135 on a surface of the silicon layer 133 opposite the titanium metal layer 129; and a metal cap layer 137 on a surface of the nickel layer 135 opposite the silicon layer 133. In one preferred embodiment, the titanium metal layer 129 is directly on the surface of the GaN/AlGaN structure 127, the silicon layer 133 is directly on the surface of the titanium metal layer 129 opposite the GaN/AlGaN structure 127, the nickel layer 135 is directly on the surface of the silicon layer 133 opposite the titanium metal layer 129, and the metal cap layer 137 is directly on the surface of the nickel layer 135 opposite the silicon layer 133.

The titanium metal layer 129 provides an ohmic contact to the GaN/AlGaN structure 127. Preferably, a thickness of the titanium metal layer 129 is in a range of and including 200 Angstroms ±5%. The nickel silicide layer 131 protects the titanium metal layer 129. The silicon layer 133 and the nickel layer 135 are selectively formed such that, during subsequent thermal annealing, the silicon layer 133 and the nickel layer 135 chemically react to form nickel silicide, which has a lower resistivity than nickel disilicide. More specifically, in order to selectively form the nickel silicide layer 131, the thicknesses of the silicon layer 133 and the nickel layer 135 are selected such that an atomic weight percentage of silicon in the silicon and nickel layers 133 and 135 is in a range of and including 45% to 60%, and more particularly, in a range of and including 48% to 52%, and even more particularly, equal to about 50%. As a result, when thermally annealed, the silicon layer 133 and the nickel layer 135 chemically react to form nickel silicide, rather than nickel disilicide. In the preferred embodiment, a thickness of the silicon layer 133 is in a range of and including 1500 Angstroms ±5%, a thickness of the nickel layer 135 is in a range of and including 750 Angstroms ±5%, and a ratio of the thickness of the silicon layer 133 to the thickness of the nickel layer 135 is, or is approximately, 2:1. As discussed below, formation of the nickel silicide layer 131 by thermally annealing the silicon layer 133 and the nickel layer 135 is performed at a temperature sufficient to form the nickel silicide layer 131 without significant chemical reaction between the titanium metal layer 129 and the silicon layer 133. As a result, the titanium metal layer 129 remains chemically unchanged and, therefore, maintains its preferred ohmic contact characteristics (e.g., low resistivity).

The metal cap layer 137 may be tellurium (Te), platinum (Pt), palladium (Pd), vanadium (V), tungsten (W), gold (Au), iridium (Ir), or rhodium (Rh). Preferably, a thickness of the metal cap layer 137 is in a range of and including 125 Angstroms ±5%. Among other things, the metal cap layer 137 protects the silicon and nickel layers 133 and 135 and/or the subsequently formed nickel silicide layer 131 from chemical attack during subsequent processing (e.g., oxidation). In the preferred embodiment, the thickness of the titanium metal layer 129 is approximately 8% (e.g., 8±0.4%) of an overall thickness of the ohmic contact structure 125, the thickness of the silicon layer 133 is approximately 58% (e.g., 58±2.9%) of the overall thickness of the ohmic contact structure 125, the thickness of the nickel layer 135 is approximately 29% (e.g., 29±1.45%) of the overall thickness of the ohmic contact structure 125, and the thickness of the metal cap layer 137 is approximately 5% (e.g., 5±0.25%) of the overall thickness of the ohmic contact structure 125.

The ohmic contact structure 125 may be chemically stable and/or corrosion resistant, and/or may provide a low resistance contact with the underlying GaN/AlGaN structure 127 while maintaining adhesion with the underlying GaN/AlGaN structure 127 over a useful life of the device. As discussed below in more detail, the useful life of the ohmic contact structure 125 is substantially improved as compared to that of traditional ohmic contacts, particularly for GaN/AlGaN devices. More specifically, the ohmic contact structure 125 experiences less than or equal to 5%, more preferably less than or equal to 2%, more preferably less than or equal to 1.5%, and even more preferably less than or equal to 1%, degradation for 1000 hours HTS at 300 degrees Celsius and/or less than or equal to 10%, more preferably less than or equal to 7.5%, more preferably less than or equal to 6%, more preferably less than or equal to 5%, and even more preferably less than or equal to 3% degradation for 1000 hours HTOL at 225 degrees Celsius and 50 mA/mm.

FIGS. 8A through 8F graphically illustrate fabrication of the ohmic contact structure 125 of FIG. 7 according to one embodiment of the present disclosure. First, as illustrated in FIG. 8A, the GaN/AlGaN structure 127 is provided. Note that, while not illustrated, the GaN/AlGaN structure 127 may be formed on a substrate, which may be a silicon substrate, a silicon carbide substrate, a sapphire substrate, or the like. For example, the substrate may be a semi-insulating silicon carbide substrate that may be, for example, the 4H polytype of silicon carbide. Other silicon carbide candidate polytypes may include the 3C, 6H, and 15R polytypes. The substrate may be a HPSI substrate, available from Cree, Inc. The term “semi-insulating” is used descriptively herein, rather than in an absolute sense.

As also shown in FIG. 8A, a photoresist lift-off mask 139 may be formed on the surface of the GaN/AlGaN structure 127, exposing portions of the surface of the GaN/AlGaN structure 127 where the ohmic contact structure 125 (FIG. 7) is to be formed. Then, layers of ohmic contact materials are formed on the photoresist lift-off mask 139 and on the exposed portions of the surface of the GaN/AlGaN structure 127 to provide the ohmic contact structure 125 of FIG. 7. While lift-off patterning is discussed by way of example in FIGS. 8A through 8F, the ohmic contact structure 125 may be formed using other operations. For example, blanket layers 129, 131, and 137 may be formed directly on the GaN/AlGaN structure 127 (i.e., without a photoresist lift-off mask) and then patterned using subsequent photolithographic masking and etch operations.

As illustrated in FIG. 8B, the titanium metal layer 129 is formed on, and preferably directly on, the surface of the photoresist lift-off mask 139 and the exposed portions of the surface of the GaN/AlGaN structure 127. The titanium metal layer 129 may be formed by, for example, evaporation or sputtering. As an example, the titanium metal layer 129 may be formed by evaporation at a rate of 4 Angstroms per second. In one preferred embodiment, the thickness of the titanium metal layer 129 is in the range of and including 200 Angstroms±5%.

Next, as illustrated in FIG. 8C, the silicon layer 133 is formed on, and preferably directly on, the titanium metal layer 129 over both the photoresist lift-off mask 139 and the portion of the surface of the GaN/AlGaN structure 127 exposed by the photoresist lift-off mask 139. Then, as illustrated in FIG. 8D, the nickel layer 135 is formed on, and preferably directly on, the surface of the silicon layer 133 opposite the titanium metal layer 129 over both the photoresist lift-off mask 139 and the portion of the surface of the GaN/AlGaN structure 127 exposed by the photoresist lift-off mask 139. The silicon layer 133 and the nickel layer 135 may be formed by, for example, evaporation or sputtering. As an example, the silicon layer 133 may be formed by evaporation at a rate of 3 Angstroms per second, and the nickel layer 135 may be formed by evaporation at a rate of 1.5 Angstroms per second. In the preferred embodiment, the silicon layer 133 and the nickel layer 135 are selectively formed such that, during subsequent thermal annealing, the silicon layer 133 and the nickel layer 135 chemically react to form nickel silicide, rather than nickel disilicide. More specifically, in one embodiment, the atomic weight ratio of silicon in the silicon and nickel layers 133 and 135 is in a range of and including 45% to 60%, and more particularly in a range of and including 48% to 52%, and even more particularly equal to approximately 50%. In one preferred embodiment, the ratio of the thickness of the silicon layer 133 to the thickness of the nickel layer 135 is, or is approximately, 2:1. In one specific embodiment, the thickness of the silicon layer 133 is in the range of and including 1500 Angstroms±5%, and the thickness of the nickel layer 135 is in the range of and including 750 Angstroms±5%.

Next, as illustrated in FIG. 8E, the metal cap layer 137 is formed on, and preferably directly on, the surface of the nickel layer 135 opposite the silicon layer 133 over both the photoresist lift-off mask 139 and the portion of the surface of the GaN/AlGaN structure 127 exposed by the photoresist lift-off mask 139. The metal cap layer 137 may be formed by, for example, evaporation or sputtering. As an example, the metal cap layer 137 may be formed by evaporation at a rate of 3 Angstroms per second. The metal cap layer 137 may be, for example, Te, Pt, Pd, V, W, Au, Ir, or Rh. In one preferred embodiment, the thickness of the metal cap layer 137 is in the range of and including 125 Angstroms±5%. Notably, the titanium metal layer 129, the silicon layer 133, the nickel layer 135, and the metal cap layer 137 may be formed in situ in a same reaction chamber.

Next, as illustrated in FIG. 8F, the photoresist lift-off mask 139 is removed (e.g., dissolved). Thermal annealing is then performed such that the silicon layer 133 and the nickel layer 135 chemically react to form the nickel silicide layer 131. Thermal annealing is performed at a temperature sufficient to form the nickel silicide layer 131 without significant chemical reaction between the titanium metal layer 129 and the silicon layer 133. Further, the silicon layer 133 reduces mixing of the titanium metal layer 129 and the nickel layer 135. More specifically, thermal annealing is performed at a temperature in a range of and including 200 degrees Celsius to 600 degrees Celsius. In one embodiment, the thermal annealing is a two-stage process including a first thermal anneal performed at a temperate in a range of and including 300 degrees Celsius to 400 degrees Celsius followed by a rapid thermal anneal at a temperature in a range of and including 400 degrees Celsius to 600 degrees Celsius. In another embodiment, the thermal annealing is a two-stage process including a first thermal anneal performed at a temperate in a range of and including 350 degrees Celsius±5% followed by a rapid thermal anneal at a temperature in a range of and including 555 degrees Celsius±5%. The first stage of the thermal anneal may be conducted for an amount of time in a range of and including 10 to 20 minutes, an amount of time in a range of and including 15 minutes±5%, or an amount of time equal to or at least substantially equal to 15 minutes. The second stage of the thermal anneal may be conducted for an amount of time in a range of and including 2 to 10 minutes.

Notably, while not illustrated, optionally, a protective layer may be formed on the ohmic contact structure 125 and exposed surfaces of the GaN/AlGaN structure 127 before or after the thermal anneal operation. The protective layer may be, for example, a layer of an insulating material such as silicon nitride (Si_(x)N_(y)), AlN, SiO₂, and/or other suitable protective material. Other materials may also be used for the protective layer. For example, the protective layer may also include magnesium oxide, scandium oxide, aluminum oxide, and/or aluminum oxynitride. Furthermore, the protective layer may be a single layer or may include multiple layers of uniform and/or non-uniform composition. The metal cap layer 137 may, in some embodiments, be removed after the thermal anneal operation and before forming the protective layer. The protective layer may then be patterned and etched using photolithographic mask and etch operation(s) to expose the ohmic contact structure 125. In some embodiments, the metal cap layer 137 may be removed after exposing the ohmic contact structure 125.

FIG. 9 illustrates the ohmic contact structure 125 according to another embodiment of the present disclosure. In this embodiment, the nickel silicide layer 131 is formed by an alternating series of silicon layers 133-1 through 133-3 and nickel layers 135-1 through 135-3. Note that while three silicon layers 133-1 through 133-3 and three nickel layers 135-1 through 135-3 are shown, the nickel silicide layer 131 of FIG. 9 may be formed from any number of two or more silicon layers and two or more nickel layers. For example, the nickel silicide layer 131 may be formed from 2 to 10 pairs of silicon and nickel layers.

As discussed above with respect of FIG. 7, the GaN/AlGaN structure 127 includes one or more layers of GaN and/or AlGaN in which one or more semiconductor devices are formed. The semiconductor devices may be, for example, HEMTs, MOSFETs, PIN diodes, bipolar junction transistors, light emitting diodes, or the like. However, one of skill in the art will readily appreciate that other types of semiconductor devices may be fabricated in the GaN/AlGaN structure 127. It should also be noted that while the present disclosure focuses on the ohmic contact structure 125 on the GaN/AlGaN structure 127 and similar Group III nitride semiconductor structures, similar ohmic contact structures may be utilized for other types of semiconductor structures such as, for example, silicon carbide semiconductor structures.

In this embodiment, the ohmic contact structure 125 includes the titanium metal layer 129 on, and preferably directly on, the surface of the GaN/AlGaN structure 127; the nickel silicide layer 131 formed by thermally annealing the alternating series of the silicon layers 133-1 through 133-3 and the nickel layers 135-1 through 135-3 on, and preferably directly on, the surface of the titanium metal layer 129 opposite the GaN/AlGaN structure 127; and a metal cap layer 137 on, and preferably directly on, a surface of the nickel silicide layer 131. The titanium metal layer 129 provides an ohmic contact to the GaN/AlGaN structure 127. Preferably, a thickness of the titanium metal layer 129 is in a range of and including 200 Angstroms±5%.

The nickel silicide layer 131 protects the titanium metal layer 129. In this embodiment, the nickel silicide layer 131 is formed by the alternating series of the silicon layers 133-1 through 133-3 and the nickel layers 135-1 through 135-3, which more specifically includes a first silicon layer 133-1 on, and preferably directly on, the surface of the titanium metal layer 129 opposite the GaN/AlGaN structure 127, a first nickel layer on, and preferably directly on, a surface of the first silicon layer 133-1 opposite the titanium metal layer 129, a second silicon layer 133-2 on, and preferably directly on, a surface of the first nickel layer 135-1 opposite the first silicon layer 133-1, a second nickel layer 135-2 on, and preferably directly on, a surface of the second silicon layer 133-1 opposite the first nickel layer 135-1, a third silicon layer 133-3 on, and preferably directly on, a surface of the second nickel layer 135-2 opposite the second silicon layer 133-2, and a third nickel layer 135-3 on, and preferably directly on, a surface of the third silicon layer 133-3 opposite the second nickel layer 135-2.

The silicon layers 133-1 through 133-3 and the nickel layers 135-1 through 135-3 are selectively formed such that, during subsequent thermal annealing, the silicon layers 133-1 through 133-3 and the nickel layers 135-1 through 135-3 chemically react to form nickel silicide, which has a lower resistivity than nickel disilicide (NiSi₂). More specifically, in order to selectively form the nickel silicide layer 131, the thicknesses of the silicon layers 133-1 through 133-3 and the nickel layers 135-1 through 135-3 are selected such that the atomic weight percentage of silicon in the silicon and nickel layers 133-1 through 133-3 and 135-1 through 135-3 is in a range of and including 45% to 60%, and more particularly, in a range of and including 48% to 52%, and even more particularly, equal to about 50%. As a result, when thermally annealed (as discussed above), the silicon layers 133-1 through 133-3 and the nickel layers 135-1 through 135-3 chemically react to form nickel silicide rather than nickel disilicide. In the preferred embodiment, a combined thickness of the silicon layers 133-1 through 133-3 is in a range of and including 1500 Angstroms±5%, a combined thickness of the nickel layers 135-1 through 135-3 is in a range of and including 750 Angstroms±5%, and a ratio of the combined thickness of the silicon layers 133-1 through 133-3 to the combined thickness of the nickel layers 135-1 through 135-3 is, or is approximately, 2:1. As discussed above, formation of the nickel silicide layer 131 by thermally annealing the silicon layers 133-1 through 133-3 and the nickel layers 135-1 through 135-3 is performed at a temperature sufficient to form the nickel silicide layer 131 without significant chemical reaction between the titanium metal layer 129 and the silicon layer 133-1. As a result, the titanium metal layer 129 remains chemically unchanged and, therefore, maintains its preferred ohmic contact characteristics (e.g., low resistivity).

The metal cap layer 137 may be Te, Pt, Pd, V, W, Au, Ir, or Rh. Preferably, a thickness of the metal cap layer 137 is in a range of and including 125 Angstroms±5%. Among other things, the metal cap layer 137 protects the silicon layers 133-1 through 133-3 and the nickel layers 135-1 through 135-3 and/or the subsequently formed nickel silicide layer 131 from chemical attack during subsequent processing (e.g., oxidation). In the preferred embodiment, the thickness of the titanium metal layer 129 is approximately 8% (e.g., 8±0.4%) of an overall thickness of the ohmic contact structure 125, the combined thickness of the silicon layers 133-1 through 133-3 is approximately 58% (e.g., 58±2.9%) of the overall thickness of the ohmic contact structure 125, the combined thickness of the nickel layers 135-1 through 135-3 is approximately 29% (e.g., 29±1.45%) of the overall thickness of the ohmic contact structure 125, and the thickness of the metal cap layer 137 is approximately 5% (e.g., 5±0.25%) of the overall thickness of the ohmic contact structure 125.

The ohmic contact structure 125 may be chemically stable and/or corrosion resistant, and/or may provide a low resistance contact with the underlying GaN/AlGaN structure 127 while maintaining adhesion with the underlying GaN/AlGaN structure 127 over a useful life of the device. As discussed below in more detail, the useful life of the ohmic contact structure 125 is substantially improved as compared to that of traditional ohmic contacts, particularly for GaN/AlGaN devices. More specifically, the ohmic contact structure 125 experiences less than or equal to 5%, more preferably less than or equal to 2%, more preferably less than or equal to 1.5%, and even more preferably less than or equal to 1% degradation for 1000 hours HTS at 300 degrees Celsius and/or less than or equal to 10%, more preferably less than or equal to 7.5%, more preferably less than or equal to 6%, more preferably less than or equal to 5%, and even more preferably less than or equal to 3% degradation for 1000 hours HTOL at 225 degrees Celsius and 50 mA/mm.

FIGS. 10A and 10B illustrate data and a corresponding graph showing percent degradation of an exemplary embodiment of the ohmic contact structure 125 of FIG. 7 after 1000 hours HTS at 300 degrees Celsius. More specifically, FIG. 10A is a table providing actual Transmission Line Method (TLM) measurements for ten of the ohmic contact structures 125 of FIG. 7 after 1000 hours HTS at 300 degrees Celsius according to one exemplary embodiment of the present disclosure. The TLM measurements were taken at a series of gap sizes, namely a 5 micron (μm) gap size, a 10 μm gap size, a 15 μm gap size, and a 20 μm gap size. After the 1000 hours HTS at 300 degrees Celsius, the percent degradation for each of the gap sizes is provided. Notably, the percent degradation is less than or equal to 10% (e.g., in a range of and including 2% to 10%), more particularly less than or equal to 7.5% (e.g., in a range of and including 2% to 7.5%), more particularly less than or equal to 6% (e.g., in a range of and including 2% to 6%), more particularly less than or equal to 5% (e.g., in a range of and including 2% to 5%), and even more particularly less than or equal to 3% (e.g., in a range of and including 2% to 3%). FIG. 10B is a graph of the TLM measurements versus gap size of FIG. 10A.

FIGS. 11A and 11B illustrate data and a corresponding graph showing percent degradation of an exemplary embodiment of the ohmic contact structure 125 of FIG. 9 after 1000 hours HTS at 300 degrees Celsius. More specifically, FIG. 11A is a table providing actual TLM measurements for ten of the ohmic contact structures 125 of FIG. 9 after 1000 hours HTS at 300 degrees Celsius according to one exemplary embodiment of the present disclosure. The TLM measurements were taken at a series of gap sizes, namely a 5 μm gap size, a 10 μm gap size, a 15 μm gap size, and a 20 μm gap size. After 1000 hours HTS at 300 degrees Celsius, the percent degradation for each of the gap sizes is provided. Notably, the percent degradation is less than or equal to 10% (e.g., in a range of and including 2% to 10%), more particularly less than or equal to 7.5% (e.g., in a range of and including 2% to 7.5%), more particularly less than or equal to 6% (e.g., in a range of and including 2% to 6%), more particularly less than or equal to 5% (e.g., in a range of and including 2% to 5%), and even more particularly less than or equal to 3% (e.g., in a range of and including 2% to 3%). FIG. 11B is a graph of the TLM measurements versus gap size of FIG. 11A.

FIGS. 12A and 12B illustrate data and a corresponding graph showing percent degradation of an exemplary embodiment of the ohmic contact structure 125 of FIGS. 7 and 9 after 1000 hours HToL at 225 degrees Celsius and 50 mA/mm. More specifically, FIG. 12A is a table providing actual TLM measurements for ten of the ohmic contact structures 125 after 1000 hours HToL at 225 degrees Celsius and 50 mA/mm according to one exemplary embodiment of the present disclosure. The TLM measurements were taken at a series of gap sizes, namely a 5 μm gap size, a 10 μm gap size, a 15 μm gap size, and a 20 μm gap size. After 1000 hours HToL at 225 degrees Celsius and 50 mA/mm, the percent degradation for each of the gap sizes is provided. Notably, the percent degradation is less than or equal to 5% (e.g., in a range of and including 0.1% to 5%), more particularly less than or equal to 2% (e.g., in a range of and including 0.1% to 2%), more particularly less than or equal to 1.5% (e.g., in a range of and including 0.1% to 1.5%), and even more particularly less than or equal to 1% (e.g., in a range of and including 0.1% to 1%). FIG. 12B is a graph of the TLM measurements versus gap size for the ohmic contact structures 125.

Those skilled in the art will recognize improvements and modifications to the preferred embodiments of the present disclosure. All such improvements and modifications are considered within the scope of the concepts disclosed herein and the claims that follow. 

1. A semiconductor device comprising: a Group Ill nitride semiconductor structure; and an ohmic contact structure on a surface of the Group Ill nitride semiconductor structure, the ohmic contact structure having less than or equal to 5% degradation after 1000 hours at 300 degrees Celsius.
 2. The semiconductor device of claim 1 wherein the ohmic contact structure has less than or equal to 2% degradation after 1000 hours at 300 degrees Celsius.
 3. The semiconductor device of claim 1 wherein the ohmic contact structure has less than or equal to 1.5% degradation after 1000 hours at 300 degrees Celsius.
 4. The semiconductor device of claim 1 wherein the ohmic contact structure has less than or equal to 1% degradation after 1000 hours at 300 degrees Celsius.
 5. The semiconductor device of claim 1 wherein the ohmic contact structure has less than or equal to 5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter.
 6. The semiconductor device of claim 1 wherein the ohmic contact structure has one of a group consisting of: less than or equal to 10% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, less than or equal to 7.5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, less than or equal to 6% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, less than or equal to 5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, and less than or equal to 3% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter.
 7. The semiconductor device of claim 1 wherein the ohmic contact structure comprises: a titanium layer on the surface of the Group III nitride semiconductor structure; a nickel silicide layer on a surface of the titanium layer opposite the Group III nitride semiconductor structure; and a metal cap layer on a surface of the nickel silicide layer opposite the titanium layer.
 8. The semiconductor device of claim 7 wherein the metal cap layer is formed of one of a group consisting of: tellurium (Te), platinum (Pt), palladium (Pd), vanadium (V), tungsten (W), gold (Au), iridium (Ir), and rhodium (Rh).
 9. The semiconductor device of claim 1 wherein the ohmic contact structure comprises: a titanium layer on the surface of the Group III nitride semiconductor structure; an alternating series of one or more silicon layers and one or more nickel layers on a surface of the titanium layer opposite the Group III nitride semiconductor structure; and a metal cap layer on a surface of the alternating series of the one or more silicon layers and the one or more nickel layers opposite the titanium layer.
 10. The semiconductor device of claim 9 wherein the alternating series of the one or more silicon layers and the one or more nickel layers comprises: a silicon layer on the surface of the titanium layer opposite the Group III nitride semiconductor structure; and a nickel layer on a surface of the silicon layer opposite the titanium layer; wherein the metal cap layer is on a surface of the nickel layer opposite the silicon layer.
 11. The semiconductor device of claim 9 wherein the alternating series of the one or more silicon layers and the one or more nickel layers comprises: a first silicon layer on the surface of the titanium layer opposite the Group III nitride semiconductor structure; a first nickel layer on a surface of the first silicon layer opposite the titanium layer; a second silicon layer on a surface of the first nickel layer opposite the first silicon layer; a second nickel layer on a surface of the second silicon layer opposite the first nickel layer; a third silicon layer on a surface of the second nickel layer opposite the second silicon layer; and a third nickel layer on a surface of the third silicon layer opposite the second nickel layer; wherein the metal cap layer is on a surface of the third nickel layer opposite the third silicon layer.
 12. The semiconductor device of claim 9 wherein the metal cap layer is formed of one of a group consisting of: tellurium (Te), platinum (Pt), palladium (Pd), vanadium (V), tungsten (W), gold (Au), iridium (Ir), and rhodium (Rh).
 13. The semiconductor device of claim 9 wherein an atomic weight percentage of silicon in the alternating series of the one or more silicon layers and the one or more nickel layers is in a range of and including 45% to 60%.
 14. The semiconductor device of claim 9 wherein a ratio of a combined thickness of the one or more silicon layers to a combined thickness of the one or more nickel layers is 2:1.
 15. The semiconductor device of claim 9 wherein a combined thickness of the one or more silicon layers is in a range of and including 1500 Angstroms±5%, and a combined thickness of the one or more nickel layers is in a range of and including 750 Angstroms±5%.
 16. The semiconductor device of claim 15 wherein a thickness of the titanium layer is in a range of and including 200 Angstroms±5%, and a thickness of the metal cap layer is in a range of and including 125 Angstroms±5%.
 17. The semiconductor device of claim 9 wherein the alternating series of the one or more silicon layers and the one or more nickel layers is an alternating series of two or more silicon layers and two or more nickel layers.
 18. The semiconductor device of claim 1 wherein the Group III nitride semiconductor structure comprises at least one of gallium nitride (GaN) and aluminum gallium nitride (AlGaN).
 19. A method of fabrication of an ohmic contact structure on a semiconductor device comprising: providing a Group III nitride semiconductor structure; and providing the ohmic contact structure on a surface of the Group III nitride semiconductor structure such that the ohmic contact structure experiences less than or equal to 5% degradation after 1000 hours at 300 degrees Celsius.
 20. The method of claim 19 wherein providing the ohmic contact structure comprises providing the ohmic contact structure on the surface of the Group III nitride semiconductor structure such that the ohmic contact structure experiences less than or equal to 2% degradation after 1000 hours at 300 degrees Celsius.
 21. The method of claim 19 wherein providing the ohmic contact structure comprises providing the ohmic contact structure on the surface of the Group III nitride semiconductor structure such that the ohmic contact structure experiences less than or equal to 1.5% degradation after 1000 hours at 300 degrees Celsius.
 22. The method of claim 19 wherein providing the ohmic contact structure comprises providing the ohmic contact structure on the surface of the Group III nitride semiconductor structure such that the ohmic contact structure experiences less than or equal to 1% degradation after 1000 hours at 300 degrees Celsius.
 23. The method of claim 19 wherein providing the ohmic contact structure comprises providing the ohmic contact structure on the surface of the Group III nitride semiconductor structure such that the ohmic contact structure experiences less than or equal to 5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter.
 24. The method of claim 19 wherein providing the ohmic contact structure comprises providing the ohmic contact structure on the surface of the Group III nitride semiconductor structure such that the ohmic contact structure experiences one of a group consisting of: less than or equal to 10% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, less than or equal to 7.5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, less than or equal to 6% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, less than or equal to 5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, and less than or equal to 3% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter.
 25. The method of claim 19 wherein providing the ohmic contact structure comprises: providing a titanium layer on the surface of the Group III nitride semiconductor structure; providing a nickel silicide layer on a surface of the titanium layer opposite the Group III nitride semiconductor structure; and providing a metal cap layer on a surface of the nickel silicide layer opposite the titanium layer.
 26. The method of claim 25 wherein the metal cap layer is formed of one of a group consisting of: tellurium (Te), platinum (Pt), palladium (Pd), vanadium (V), tungsten (W), gold (Au), iridium (Ir), and rhodium (Rh).
 27. The method of claim 19 wherein providing the ohmic contact structure comprises: providing a titanium layer on the surface of the Group III nitride semiconductor structure; providing an alternating series of one or more silicon layers and one or more nickel layers on a surface of the titanium layer opposite the Group III nitride semiconductor structure; providing a metal cap layer on a surface of the alternating series of the one or more silicon layers and the one or more nickel layers opposite the titanium layer; and annealing the ohmic contact structure such that the alternating series of the one or more silicon layers and the one or more nickel layers form a nickel silicide layer.
 28. The method of claim 27 wherein providing the alternating series of the one or more silicon layers and the one or more nickel layers comprises: providing a silicon layer on the surface of the titanium layer opposite the Group III nitride semiconductor structure; and providing a nickel layer on a surface of the silicon layer opposite the titanium layer; wherein providing the metal cap layer on the surface of the alternating series of the one or more silicon layers and the one or more nickel layers opposite the titanium layer comprises providing the metal cap layer on a surface of the nickel layer opposite the silicon layer.
 29. The method of claim 27 wherein providing the alternating series of the one or more silicon layers and the one or more nickel layers comprises: providing a first silicon layer on the surface of the titanium layer opposite the Group III nitride semiconductor structure; providing a first nickel layer on a surface of the first silicon layer opposite the titanium layer; providing a second silicon layer on a surface of the first nickel layer opposite the first silicon layer; providing a second nickel layer on a surface of the second silicon layer opposite the first nickel layer; providing a third silicon layer on a surface of the second nickel layer opposite the second silicon layer; and providing a third nickel layer on a surface of the third silicon layer opposite the second nickel layer; wherein providing the metal cap layer on the surface of the alternating series of the one or more silicon layers and the one or more nickel layers opposite the titanium layer comprises providing the metal cap layer on a surface of the third nickel layer opposite the third silicon layer.
 30. The method of claim 27 wherein the metal cap layer is formed of one of a group consisting of: tellurium (Te), platinum (Pt), palladium (Pd), vanadium (V), tungsten (W), gold (Au), iridium (Ir), and rhodium (Rh).
 31. The method of claim 27 wherein an atomic weight percentage of silicon in the alternating series of the one or more silicon layers and the one or more nickel layers is in a range of and including 45% to 60%.
 32. The method of claim 27 wherein a ratio of a combined thickness of the one or more silicon layers to a combined thickness of the one or more nickel layers is 2:1.
 33. The method of claim 27 wherein a combined thickness of the one or more silicon layers is in a range of and including 1500 Angstroms±5%, and a combined thickness of the one or more nickel layers is in a range of and including 750 Angstroms±5%.
 34. The method of claim 33 wherein a thickness of the titanium layer is in a range of and including 200 Angstroms±5%, and a thickness of the metal cap layer is in a range of and including 125 Angstroms±5%.
 35. The method of claim 27 wherein the alternating series of the one or more silicon layers and the one or more nickel layers is an alternating series of two or more silicon layers and two or more nickel layers.
 36. The method of claim 27 wherein annealing the ohmic contact structure comprises annealing the ohmic contact structure at a temperature at or below 600 degrees Celsius.
 37. The method of claim 27 wherein annealing the ohmic contact structure comprises: annealing the ohmic contact structure at a first temperature in a range of and including 200 degrees Celsius to 400 degrees Celsius such that the alternating series of the one or more silicon layers and the one or more nickel layers form the nickel silicide layer; and annealing the ohmic contact structure at a second temperature that is higher than the first temperature and in a range of and including 500 degrees Celsius to 600 degrees Celsius to finalize the ohmic contact structure.
 38. The method of claim 19 wherein the Group Ill nitride semiconductor structure comprises at least one of gallium nitride (GaN) and aluminum gallium nitride (AlGaN).
 39. A semiconductor device comprising: a Group Ill nitride semiconductor structure; and an ohmic contact structure on a surface of the Group Ill nitride semiconductor structure, the ohmic contact structure having less than or equal to 10% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter.
 40. The semiconductor device of claim 39 wherein the ohmic contact structure has less than or equal to 7.5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter.
 41. The semiconductor device of claim 39 wherein the ohmic contact structure has less than or equal to 5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter.
 42. The semiconductor device of claim 39 wherein the ohmic contact structure has one of a group consisting of: less than or equal to 7.5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, less than or equal to 6% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, less than or equal to 5% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter, and less than or equal to 3% degradation after 1000 hours at 225 degrees Celsius and 50 milliamps per millimeter. 